In vitro and in vivo degradation of poly(1,3-diamino-2-hydroxypropane-co-polyol sebacate) elastomers

被引:31
作者
Bettinger, Christopher J. [3 ,4 ]
Bruggeman, Joost P. [1 ,2 ]
Borenstein, Jeffrey T. [3 ]
Langer, Robert [1 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] Erasmus Univ, Erasmus Med Ctr, Dept Plast & Reconstruct Surg, NL-3015 GE Rotterdam, Netherlands
[3] Charles Stark Draper Lab Inc, Ctr Biomed Engn, Cambridge, MA 02139 USA
[4] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
关键词
elastomer; tissue engineering; biodegradable; BIODEGRADABLE ELASTOMERS; BEHAVIOR; STAR-POLY(EPSILON-CAPROLACTONE-CO-D; L-LACTIDE); RELEASE;
D O I
10.1002/jbm.a.32306
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Biomaterials with a wide range of tunable properties are desirable for application-specific Purposes. We have previously developed a class of elastomeric poly(ester amides) based on the amine alcohol 1,3-diamino-2-hydroxypropane termed poly(1,3-diamino-2-hydroxypropane-co-polyol sebacate) or APS. In this work, we have synthesized and characterized formulations of APS polymers and studied the degradation of these polymers in vitro and in vivo. It was found that the chemical, physical, and mechanical properties of APS polymers could be tuned by adjusting monomer feed ratios and polymerization conditions. The degradation kinetics could also be greatly influenced by altering the formulation of APS polymers. hi vivo degradation half-lives ranged from 6 to similar to 100 weeks. Furthermore, the dominant degradation mechanism (i.e. hydrolytic or enzymatic) could be controlled by adjusting the specific formulation of the APS polymer. On the basis of the observed in vitro and in vivo biodegradation phenomena, we also propose that the primary modes of degradation are composition dependent. (C) 2008 Wiley periodicals, Inc. J Biomed Mater Res 91A: 1077-1088, 2009
引用
收藏
页码:1077 / 1088
页数:12
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